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Tryptamine ester

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Identification
Molecular formula
C18H17N3O2
CAS number
NA
IUPAC name
[3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate
State
State

At room temperature, [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate is in a solid state. It is stable under standard conditions, although it should be stored away from light and moisture to prevent degradation.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
306.35g/mol
Molar mass
306.3500g/mol
Density
1.3000g/cm3
Appearence

[3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate typically appears as a white to off-white crystalline powder. Its purity and texture can vary slightly depending on the method of synthesis and the presence of impurities.

Comment on solubility

Solubility of [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate

The solubility of [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate is a fascinating aspect that can be influenced by various factors. Understanding solubility is crucial for applications in pharmaceuticals, agrochemicals, and material science. Here are some key points to consider:

  • Polar vs. Nonpolar Characteristics: This compound possesses both polar and nonpolar functional groups, indicating that its solubility may vary significantly in different solvents.
  • Solvent Types:
    • Aqueous Solubility: It is likely to have moderate solubility in water due to the presence of amino and carboxylate groups, which can engage in hydrogen bonding.
    • Organic Solvents: The pyridine and indole rings suggest better solubility in polar organic solvents like methanol and ethanol.
  • Temperature Influence: Increased temperature generally enhances solubility, which may be beneficial for dissolution in both aqueous and organic systems.
  • pH Sensitivity: The solubility could also be sensitive to pH changes; for instance, a more acidic medium might affect the carboxylate ionization, impacting overall solubility.

Due to these multifaceted interactions, it is essential to conduct empirical tests to establish precise solubility values for [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate in various solvents to fully comprehend its behavior in practical applications.

Interesting facts

Interesting Facts about [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate

As a fascinating compound, [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate possesses unique properties and applications that intrigue both chemists and biologists. Here are some noteworthy points:

  • Biological Significance: This compound is of particular interest in medicinal chemistry due to its structural similarity to various neurotransmitters and has potential implications in the study of neurological conditions.
  • Research Applications: It serves as a valuable intermediate in organic synthesis and is actively researched for its roles in pharmaceuticals, particularly in developing new therapeutic agents.
  • Indole Framework: The indole unit within its structure is known for being a precursor in many biologically active compounds, which may contribute to its potential effectiveness as a drug.
  • Pyridine Influence: The presence of the pyridine ring enhances its electron-accepting properties, which could facilitate interactions within biological systems.
  • Aminoethyl Linkage: The aminoethyl group allows for further modifications and the potential for creating a range of derivatives, expanding its applications in drug development.

In summary, [3-(2-aminoethyl)-1H-indol-5-yl] pyridine-4-carboxylate stands out due to its intricate structure and noteworthy interactions with biological systems. The ongoing research in this area opens up exciting pathways for new discoveries and advancements in chemistry.